Variant report

Variant	nsv966780
Chromosome Location	chr7:38374343-38407875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2260)
CpG islands
(count:610)
Chromatin interactive
region (count:22)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38380924-38381236	K562	blood:	n/a	n/a
2	ARID3A	chr7:38375261-38375775	K562	blood:	n/a	n/a
3	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
4	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
5	ATF1	chr7:38375958-38376139	K562	blood:	n/a	n/a
6	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
7	ATF1	chr7:38375268-38375593	K562	blood:	n/a	n/a
8	ATF2	chr7:38375154-38375534	GM12878	blood:	n/a	n/a
9	ATF2	chr7:38375126-38375565	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:38375250-38375572	K562	blood:	n/a	n/a
11	ATF3	chr7:38375159-38375625	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:38375296-38375468	K562	blood:	n/a	n/a
13	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
14	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
15	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
16	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
17	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
18	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
19	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
20	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
21	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
22	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
23	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
24	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
25	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
26	BATF	chr7:38375071-38375552	GM12878	blood:	n/a	n/a
27	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
28	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
29	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
30	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
31	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
32	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
35	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
36	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
37	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
38	BCL3	chr7:38375082-38375686	A549	lung:	n/a	chr7:38375198-38375207
39	BCLAF1	chr7:38375115-38375667	GM12878	blood:	n/a	chr7:38375198-38375207
40	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
41	BCLAF1	chr7:38375138-38375654	GM12878	blood:	n/a	chr7:38375198-38375207
42	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
43	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:38375174-38375547	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
50	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398836-38398886	MCF10A-Er-Src	breast:	n/a
2	chr7:38375485-38375535	HRPEpiC	eye:	n/a
3	chr7:38389659-38389709	NB4	blood:	n/a
4	chr7:38398839-38398889	CMK	blood:	n/a
5	chr7:38389991-38390041	Hepatocyte	liver:	n/a
6	chr7:38389659-38389709	BJ	skin:	n/a
7	chr7:38389685-38389735	HRPEpiC	eye:	n/a
8	chr7:38389991-38390041	HRCEpiC	kidney:	n/a
9	chr7:38398839-38398889	SK-N-MC	brain:	n/a
10	chr7:38389685-38389735	SKMC	muscle:	n/a
11	chr7:38389685-38389735	RPTEC	kidney:	n/a
12	chr7:38375376-38375426	HNPCEpiC	eye:	n/a
13	chr7:38403507-38403557	NHBE	bronchial:	n/a
14	chr7:38389991-38390041	RPTEC	kidney:	n/a
15	chr7:38375485-38375535	HCF	heart:	n/a
16	chr7:38403507-38403557	HCF	heart:	n/a
17	chr7:38389685-38389735	AG09309	skin:	n/a
18	chr7:38389991-38390041	Caco-2	colon:	n/a
19	chr7:38380582-38380632	K562	blood:	n/a
20	chr7:38398836-38398886	HMEC	breast:	n/a
21	chr7:38389685-38389735	HUVEC	blood vessel:	n/a
22	chr7:38380582-38380632	HUVEC	blood vessel:	n/a
23	chr7:38389659-38389709	HEEpiC	esophagus:	n/a
24	chr7:38375485-38375535	NHDF-neo	bronchial:	n/a
25	chr7:38398836-38398886	ovcar-3	ovarian:	n/a
26	chr7:38380487-38380537	HEK293	kidney:	embryo
27	chr7:38380487-38380537	GM12892	blood:	n/a
28	chr7:38389991-38390041	GM12892	blood:	n/a
29	chr7:38398836-38398886	HEEpiC	esophagus:	n/a
30	chr7:38398839-38398889	PFSK-1	brain:	n/a
31	chr7:38389685-38389735	NHBE	bronchial:	n/a
32	chr7:38398839-38398889	GM12891	blood:	n/a
33	chr7:38380487-38380537	HRCEpiC	kidney:	n/a
34	chr7:38389659-38389709	SK-N-SH	brain:	n/a
35	chr7:38398839-38398889	HEK293	kidney:	embryo
36	chr7:38389991-38390041	HRE	kidney:	n/a
37	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
38	chr7:38389685-38389735	LNCaP	prostate:	n/a
39	chr7:38398836-38398886	SKMC	muscle:	n/a
40	chr7:38375485-38375535	MCF-7	breast:	n/a
41	chr7:38389659-38389709	Hela-S3	cervix:	n/a
42	chr7:38375485-38375535	AG04449	skin:	fetal
43	chr7:38403507-38403557	AG09319	gingival:	n/a
44	chr7:38375376-38375426	HL-60	blood:	n/a
45	chr7:38375376-38375426	AoSMC	blood vessel:	n/a
46	chr7:38389659-38389709	HUVEC	blood vessel:	n/a
47	chr7:38375485-38375535	AoSMC	blood vessel:	n/a
48	chr7:38380582-38380632	GM19239	blood:	n/a
49	chr7:38375376-38375426	HAEpiC	amniotic membrane:	n/a
50	chr7:38398836-38398886	HRE	kidney:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38269978..38272526-chr7:38377435..38379545,2	K562	blood:
2	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
3	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
4	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
5	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
6	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
7	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
8	chr7:38369664..38372472-chr7:38373590..38376789,3	K562	blood:
9	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
10	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
11	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
12	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
13	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
14	chr7:38255022..38255645-chr7:38375302..38376120,3	MCF-7	breast:
15	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
16	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
17	chr7:38375472..38376033-chr7:38384935..38385704,2	MCF-7	breast:
18	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
19	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
20	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
21	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
22	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
2	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
3	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
4	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179
5	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
6	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
7	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
8	lnc-AMPH-5	chr7:38374642-38374951	NONHSAT120177
9	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
10	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
11	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
12	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
13	lnc-AMPH-5	chr7:38375073-38375115	NONHSAT120177
14	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
15	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
16	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
17	lnc-AMPH-1	chr7:38407614-38407746	XLOC_006412
18	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178
19	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
20	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924

No data

Variant related genes	Relation type
TRGV2	TF binding region
TRGV7	TF binding region
TRGV5	TF binding region
TRGV1	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV8	TF binding region
TRGV5P	TF binding region
TRGV2	CpG island
TRGV7	CpG island
TRGV5	CpG island
TRGV1	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV8	CpG island
TRGV5P	CpG island
ENSG00000228668	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000211698	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000211701	chromatin interactions
SERTAD3	miRNA target sites
CA13	miRNA target sites
RAB5A	miRNA target sites

Extended variants
information (count: 2066 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2066 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148304112	chr7:38374347-38374348	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs185214188	chr7:38374358-38374359	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs74391596	chr7:38374377-38374378	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs190763029	chr7:38374432-38374433	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs183361514	chr7:38374436-38374437	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs548457840	chr7:38374444-38374445	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs2240852	chr7:38374456-38374457	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568674014	chr7:38374476-38374477	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs141428701	chr7:38374518-38374519	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs533354090	chr7:38374543-38374544	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs56369268	chr7:38374589-38374590	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs570569188	chr7:38374604-38374605	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs187215754	chr7:38374609-38374610	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs556238976	chr7:38374639-38374640	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs576233998	chr7:38374652-38374653	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs554310184	chr7:38374660-38374661	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs2240853	chr7:38374697-38374698	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs193164226	chr7:38374703-38374704	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs572178186	chr7:38374728-38374729	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs376643044	chr7:38374744-38374745	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs560174300	chr7:38374787-38374788	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs576279142	chr7:38374788-38374789	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs368717780	chr7:38374792-38374793	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs532510121	chr7:38374827-38374828	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs113761823	chr7:38374864-38374865	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs545790912	chr7:38374944-38374945	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs2240854	chr7:38374996-38374997	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs531897485	chr7:38374997-38374998	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs548830443	chr7:38375022-38375023	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs562269878	chr7:38375023-38375024	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs527842677	chr7:38375072-38375073	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs548048417	chr7:38375119-38375120	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs570556790	chr7:38375138-38375139	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs2735160	chr7:38375210-38375211	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs549786019	chr7:38375257-38375258	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs558595444	chr7:38375261-38375262	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs535125994	chr7:38375295-38375296	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs555589255	chr7:38375313-38375314	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs572260722	chr7:38375314-38375315	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs150477989	chr7:38375322-38375323	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs373059243	chr7:38375325-38375326	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs557579630	chr7:38375327-38375328	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs10249867	chr7:38375337-38375338	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs541171871	chr7:38375384-38375385	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs183626449	chr7:38375445-38375446	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs559975115	chr7:38375471-38375472	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs576359629	chr7:38375485-38375486	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs541864677	chr7:38375509-38375510	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs62445000	chr7:38375575-38375576	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs188173919	chr7:38375633-38375634	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38366800-38375200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:38369200-38375400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:38370400-38374800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr7:38371000-38374400	Weak transcription	Adipose Nuclei	Adipose
5	chr7:38371000-38374400	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:38371000-38375200	Weak transcription	Primary T cells from cord blood	blood
7	chr7:38371000-38375200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr7:38371000-38375400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:38371000-38375400	Weak transcription	Lung	lung
10	chr7:38371200-38374600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr7:38371200-38375200	Active TSS	Primary T cells fromperipheralblood	blood
12	chr7:38371600-38374800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:38371600-38375200	Weak transcription	A549	lung
14	chr7:38371800-38380600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr7:38372000-38374400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr7:38372000-38374800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr7:38372000-38375000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr7:38372800-38374400	Weak transcription	Fetal Intestine Large	intestine
19	chr7:38372800-38375000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:38373000-38374400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr7:38373000-38374800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr7:38373400-38375400	Weak transcription	Gastric	stomach
23	chr7:38373600-38374400	Weak transcription	Primary B cells from cord blood	blood
24	chr7:38373800-38374600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr7:38373800-38374600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:38373800-38376000	Flanking Active TSS	Dnd41	blood
27	chr7:38374000-38375000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr7:38374200-38374400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr7:38374200-38374400	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr7:38374200-38374600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:38374200-38374600	Enhancers	GM12878-XiMat	blood
32	chr7:38374200-38374800	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr7:38374200-38374800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:38374200-38375200	Active TSS	Thymus	Thymus
35	chr7:38374200-38375400	Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr7:38374200-38375400	Enhancers	K562	blood
37	chr7:38374200-38375600	Flanking Active TSS	Fetal Thymus	thymus
38	chr7:38374200-38375600	Enhancers	Spleen	Spleen
39	chr7:38374200-38377000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:38374200-38377600	Enhancers	Placenta	Placenta
41	chr7:38374400-38374600	Enhancers	Primary B cells from cord blood	blood
42	chr7:38374400-38374600	Flanking Active TSS	Primary hematopoietic stem cells	blood
43	chr7:38374400-38374800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr7:38374400-38375000	Enhancers	Adipose Nuclei	Adipose
45	chr7:38374400-38375400	Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr7:38374400-38375400	Enhancers	Fetal Intestine Large	intestine
47	chr7:38374400-38375400	Active TSS	Rectal Mucosa Donor 29	rectum
48	chr7:38374400-38375600	Enhancers	Fetal Intestine Small	intestine
49	chr7:38374400-38376000	Enhancers	Fetal Muscle Leg	muscle
50	chr7:38374600-38374800	Enhancers	Primary hematopoietic stem cells	blood

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